HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164317Generated: November 1, 2026
Styrene → Benzene, ethenyl-, polymer with 1,3-butadiene
https://huagongshe.com/reaction/2164317
Participants
| Role | Name | HCID | Charge |
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| Reactant | Styrene | HCID 7501 | — |
| Reactant | 1,3-Butadiene | HCID 7845 | — |
| Reactant | CID 53628100 | HCID 178418400 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Benzene, ethenyl-, polymer with 1,3-butadiene | HCID 62697 | — |
Reaction Steps
A one gallon reactor containing 2,000 g. of purified cyclohexane was readied for polymerization of monomer as in Example I. Into the closed reactor was charged 8.86 m moles of sec-butyllithium and 132.9 of styrene and the reactor held at 60° C. for 20 minutes. The Mn was 15,000 for the resulting polystyrene blocks. At this point, 132.9 g. of butadiene were added and the whole mixture held at 60° C. for 75 minutes to form diblock arms of 50/50 wt-% styrene/butadiene and having average Mn of 30,000. There was then added either 17.72 m moles (coupling agent/RLi=2), 26.58 m moles (coupling agent/RLi=3), 35.44 m moles (coupling agent/RLi=4), or 53.16 m moles (coupling agent/RLi=6), of the desired linking agent and the temperature held at 30° C. to complete the linking reaction. After termination and separation of the polymeric product the results shown in Table I were obtained for unlinked diblock (DB), linked triblock (TB) and starblock.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04503188 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-84337175e5db4a1195f07a00191098d6 |
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| Source note | uspto-grants-1985_03 |
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